For many years, treatment of chronic lower back pain, intervertebral disc d
egeneration, spinal fusion, and spinal cord injury have been problematic. T
he advances in molecular biology have now made it possible to address these
problems at a molecular level. By gene therapy, a defective gene is replac
ed with a normal or therapeutic gene. To be successful, the exact sequence
and function of the specific gene must be understood, a vehicle for safe an
d efficient delivery of the gene into the cells must be located, and the ex
pression of the gene should be well controlled. Until now, difficulties wit
h efficient gene transfer and appropriate gene expression have still been a
n impediment. Besides, ethical problems of a carcinogenic and eugenic natur
e have arisen [15], but with gene transfer as drug delivery system, there i
s a great range of applications to acquired diseases. Research is also bein
g conducted into various aspects of spinal disorders.